GUDIDData
eudamed_udi Primary ID: M294CM0190910

Standard cannula power wash kit, replacement male luer lock handle only (UDI M294CM0190910)

Manufactured by CLINIMED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Standard cannula power wash kit, replacement male luer lock handle only - Primary ID M294CM0190910

Device Regulatory Overview

The Standard cannula power wash kit, replacement male luer lock handle only (Model/Catalog Number: CM019091) is a medical device manufactured by CLINIMED. This product is indexed under FDA Product Code / Category Classification Y093399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CM019091
Product Code / EMDN
Y093399
Device Name
Standard cannula power wash kit, replacement male luer lock handle only
Database Sync Date
2026-08-09 16:29:40

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Standard cannula power wash kit, replacement male luer lock handle only?

The registered manufacturer of record for Standard cannula power wash kit, replacement male luer lock handle only is CLINIMED.

What is the Primary UDI-DI identifier for Standard cannula power wash kit, replacement male luer lock handle only?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M294CM0190910.

What classification code is assigned to this device?

This device is registered under product classification code Y093399.

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